A major objective of the proposed research program is to identify the subcellular basis of abnormalities that affect visual adaptation in inherited night-blinding retinal disorders. The thesis we propose to examine is that some disorders of this type are manifestations of an aberration in the processes by which the visual cell renews its molecular constituents (e.f., disc lamellae, synaptic vesicles, and other membrane-bound organelles), and that an early stage in the pathogenesis of the disease involves a disruption of the normal cytoskeletal architecture, in particular, the microtubular system. Accordingly, we propose to study with immunocytochemical and ultrastructural methods the organization of the microtubular system in photoreceptors of the cat retina, and to determine the effects on structure and synaptic transmission of the microtubule-disrupting agent, vincristine. Similar methods will be used to examine the cytoskeletal elements of visual cells in animal models of hereditary retinal disorders, namely, the night-blind Appaloosa horse, and two species of dog affected with late-onset progressive retinal atrophy (miniature poodle and Tibetan terrier). In addition, we will attempt to determine changes in rhodopsin density and visual sensitivity (and the relationship between these parameters) at various stages in the progressive disease affecting the Tibetan terrier. Because electroretinography has assumed an important role in detection of the widespread retinal dysfunction associated with hereditary retinal disease, we plan to conduct a component analysis of the ERG designed to provide information on the cellular elements that contribute to the complex waveform of the response. Lastly, intracellular studies are to be performed on isolated Muller cells from the cat retinal to determine those membrane properties that relate to the putative roles of the retinal glia in the generation of components of the ERG, and in maintaining a stable extracellular environment for neuronal function.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY006516-06
Application #
3262787
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1985-10-01
Project End
1990-12-31
Budget Start
1990-01-01
Budget End
1990-12-31
Support Year
6
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Illinois at Chicago
Department
Type
Schools of Medicine
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
Qian, Haohua; Shah, Manthan R; Alexander, Kenneth R et al. (2008) Two distinct processes are evident in rat cone flicker ERG responses at low and high temporal frequencies. Exp Eye Res 87:71-5
Chappell, Richard L; Anastassov, Ivan; Lugo, Prospero et al. (2008) Zinc-mediated feedback at the synaptic terminals of vertebrate photoreceptors. Exp Eye Res 87:394-7
Ramsey, David J; Ripps, Harris; Qian, Haohua (2007) Streptozotocin-induced diabetes modulates GABA receptor activity of rat retinal neurons. Exp Eye Res 85:413-22
Zhu, Yujie; Ripps, Harris; Qian, Haohua (2007) A single amino acid in the second transmembrane domain of GABA rho receptors regulates channel conductance. Neurosci Lett 418:205-9